A clinical study between transverse abdominis plane block and quadratus lumborum block for pain management in Caesarean Section operation.
Not Applicable
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2022/08/044599
- Lead Sponsor
- Dr Ananya Devi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA physical status 2
2. Normal singleton pregnancy with a gestational period of minimum 37 weeks
3. Elective caesarean section under spinal anaesthesia
4. Informed and written consent
Exclusion Criteria
1.Patient not willing to give consent
2.Patient belonging to ASA physical status 3 or more
3.Allergy to study drugs
4.Infection at the site of block
5.Patient with known coagulopathy or patients on anticoagulation therapy
6.Patient with pregnancy induced hypertension
7.Patient with gestational diabetes mellitus
8.Patient with fetal distress
9.Patient with cardiac disease
10.Patient with kidney disease
11.Patient with morbid obesity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of analgesia in each group after administration of block in the post operative periodTimepoint: Analgesia will be assessed at 2,4,6,12,24 post operative hours
- Secondary Outcome Measures
Name Time Method 1. To compare the total number of analgesic dose required over a period of 24 hours. <br/ ><br>2. To compare the severity of post operative pain assessment via numerical rating scale.Timepoint: Analgesia will be assessed at 2,4,6,12,24 post operative hours